AmnioMAX ™ -II Complete Medium - Indonesia BPOM Medical Device Registration
AmnioMAX ™ -II Complete Medium is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10202420003. The device is manufactured by LIFE TECHNOLOGIES CORPORATION from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. NUTRILAB PRIMARY.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LIFE TECHNOLOGIES CORPORATIONCountry of Origin
United States
Authorized Representative
PT. NUTRILAB PRIMARYAR Address
JL. RAYA KEBAYORAN LAMA NO. 18
Registration Date
Jun 30, 2024
Expiry Date
Dec 31, 2025
Product Type
Cell and Tissue Culture Products
Cell and tissue culture supplies and equipment.
Invitro Diagnostics
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